The first written record of the term floral color change was in 1877 when Charles Darwin (12 February 1809 – 19 April 1882) forwarded a letter from his colleague, naturalist Fritz Müller (31 March 1821 – 21 May 1897) to the British multidisciplinary science journal, Nature. Müller documented the patterns and efficiency of pollination in relation to the floral color change that occurred in Lantana flowers found in Brazilian forests. It is now understood that floral color change has evolved independently several times and has maintained morphological and physiological differences across taxa.
Although this phenomenon was first mentioned over 200 years ago, research on its biological relevance has only occurred within the last few decades.
The three major pigments involved in floral color change are anthocyanins, carotenoids, and betalains. Color changes can occur from any of the following; an accumulation or loss of anthocyanins, accumulation or loss of carotenoids, or an accumulation of betalains. Floral color change may also be caused by an increase or decrease in pH causing a reddening/blueing of anthocyanins and co-pigments.
Floral color change can be inducible or non-inducible. Some flowers will change color at the same rate regardless of pollinator visitation, while others can be induced by pollen deposition on the stigma. However, inducible flowers will eventually change color due to senescence even without pollinator activity.
Depending on the species, floral color change can affect an entire flower or it can occur in localized parts. Previous research has found that moth-pollinated flowers are more likely to have whole flower color changes, while other insect-pollinated flowers are more likely to have localized color changes.
While flowers typically wilt after pollination, many angiosperm taxa maintain their flowers even after their sexual viability has come to an end. During this time, flowers that have been successfully pollinated and have reduced rewards may undergo color changes, which act as a signal to their pollinators. Insect pollinators preferentially visit flowers that are sexually viable and have not undergone color change. Pollinators will learn and discriminate against floral stages from these signals benefiting both parties by allowing insects to be guided to flowers that are rewarding, while the flowers receive pollination.
It has been shown that the size of the plant's floral display is important in relation to plant-pollinator interactions. Larger floral displays are more likely to be seen and visited by their pollinators than small inconspicuous floral displays. Several angiosperm species are known to increase their floral display without producing additional flowers. These species accomplish this by retaining the older, nonfunctional flowers that would often be abscised in other species to reduce the cost to the plant that comes from the carbohydrates needed and the water loss that occurs when maintaining these tissues. However, when these flowers are retained on insect pollinated plants there are the potential benefits of enhanced reproductive success through increased pollen deposition on stigmas and export of pollen to fertilize the ovules of other plants.
Other forms of floral color change Edit
Senescence is one of the main causes of floral color change along with induction by pollination. While angiosperm taxa show variation in the time that it takes senescence to occur, the mechanism is typically associated with the biosynthesis of anthocyanins. Evening primrose in the genus Oenothera are a common example of flowers that undergo color changes due to senescence. Oenothera will bloom in the evening and appear to be white or yellow, and by morning they fade to pink or orange.
Floral color change can also be a result of an increase or decrease in pH. Hydrangea is a model genus for this particular chemical change in flowers. Floral pigments in Hydrangea are affected by the presence of aluminum ions in the soil, causing changes in flower color from red, pink, blue, light purple or dark purple.
See also Edit
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- Malloy, Mike (2017-04-15). "Morning glory's beauty part of glorious morning, colorful day". Naples Daily News.
- Ruxton, Graeme D; Schaefer, H Martin (August 2016). "Floral colour change as a potential signal to pollinators". Current Opinion in Plant Biology. 32: 96–100. doi:10.1016/j.pbi.2016.06.021. ISSN 1369-5266. PMID 27428780.
- "Hydrangea Questions and Answers". 2013-05-16. Archived from the original on 2013-05-16. Retrieved 2020-05-11.
- Weiss, Martha R. (November 1991). "Floral colour changes as cues for pollinators". Nature. 354 (6350): 227–229. Bibcode:1991Natur.354..227W. doi:10.1038/354227a0. ISSN 0028-0836. S2CID 4363595.
- Jones, C. Eugene; Cruzan, Mitchell B. (February 1999). "Floral morphological changes and reproductive success in deer weed (Lotus scoparius , Fabaceae)". American Journal of Botany. 86 (2): 273–277. doi:10.2307/2656943. ISSN 0002-9122. JSTOR 2656943.
- Weiss, Martha R.; Lamont, Byron B. (1997-05-13). "Floral Color Change and Insect Pollination: A Dynamic Relationship". Israel Journal of Plant Sciences. 45 (2–3): 185–199. doi:10.1080/07929978.1997.10676683. ISSN 0792-9978.
- Gori, David F. (July 1989). "Floral Color Change in Lupinus argenteus (Fabaceae): Why Should Plants Advertise the Location of Unrewarding Flowers to Pollinators?". Evolution. 43 (4): 870–881. doi:10.2307/2409314. ISSN 0014-3820. JSTOR 2409314. PMID 28564205.
- Cruzan, Mitchell B.; Neal, Paul R.; Willson, Mary F. (May 1988). "Floral Display in Phyla Incisa: Consequences for Male and Female Reproductive Success". Evolution. 42 (3): 505–515. doi:10.2307/2409035. ISSN 0014-3820. JSTOR 2409035. PMID 28564003.
- Teppabut, Yada; Oyama, Kin-ichi; Kondo, Tadao; Yoshida, Kumi (2018-07-12). "Change of Petals′ Color and Chemical Components in Oenothera Flowers during Senescence". Molecules. 23 (7): 1698. doi:10.3390/molecules23071698. ISSN 1420-3049. PMC 6099532. PMID 30002287.